dc.contributor.author |
Enriquez, RG |
|
dc.contributor.author |
Barajas, J |
|
dc.contributor.author |
Ortiz, B |
|
dc.contributor.author |
Lough, AJ |
|
dc.contributor.author |
Reynolds, WF |
|
dc.contributor.author |
Yu, M |
|
dc.contributor.author |
Leon, I |
|
dc.contributor.author |
Gnecco, D |
|
dc.date.accessioned |
2011-01-22T10:27:58Z |
|
dc.date.available |
2011-01-22T10:27:58Z |
|
dc.date.issued |
1997 |
|
dc.identifier.issn |
0008-4042 |
|
dc.identifier.uri |
http://hdl.handle.net/11154/3372 |
|
dc.description.abstract |
The crystal structure of monoginoic acid, 3, is determined acid compared with previously reported structures of kauradienoic acid, 1, acid kaurenoic acid, 2. H-1 and C-13 chemical shifts are assigned for all three diterpenes and solution and crystal structure conformations are confirmed with the aid of solution NOE measurements. The overall shapes of 2 and 3 are very similar while 1 is significantly dissimilar. These differences may be partially responsible for the reported greater in vitro uterotropic activity of 1, relative to 2 and 3. |
en_US |
dc.language.iso |
en |
en_US |
dc.title |
Comparison of crystal and solution structures and H-1 and C-13 chemical shifts for grandiflorenic acid, kaurenoic acid, and monoginoic acid |
en_US |
dc.type |
Article |
en_US |
dc.identifier.idprometeo |
2975 |
|
dc.source.novolpages |
75(3):342-347 |
|
dc.subject.wos |
Chemistry, Multidisciplinary |
|
dc.description.index |
WoS: SCI, SSCI o AHCI |
|
dc.subject.keywords |
monoginoic acid |
|
dc.subject.keywords |
kaurodienoic acid |
|
dc.subject.keywords |
kaurenoic acid |
|
dc.relation.journal |
Canadian Journal of Chemistry-Revue Canadienne De Chimie |
|